A Dual-Tone Multifrequency Receiver Using Synchronous Additions and Subtractions

This paper describes a new detection algorithm for a dualtone multifrequency (DTMF) signal. The new algorithm basically uses only additions and subtractions but no multiplications. A signaling tone can be detected by sampling an input signal at four times each frequency involved in a signaling tone and accumulating these sampled values synchronously by additions and subtractions. This algorithm is referred to as the synchronous additions and subtractions (SAS) method. Many conventional methods have used various types of filters to detect signaling tones. In the SAS method in which the design of filters is unnecessary, only the generation of sampling pulses is required, and main operations are additions and subtractions. These features are useful to implement flexible receivers and various types of receivers. The simplicity of the SAS method is demonstrated by the implementation of a DTMF receiver using a conventional 8-bit microcomputer without any special hardware. The minimum signal-to-noise ratio is 5.7 dB when the receiver operates for the signaling tones to be accepted. Four easily measurable parameters are used to distinguish signaling tones from noise inputs. Only two false detections occurred for severe noise inputs of thirty hours.     

Electrical property and defect structure of lanthanum-doped polycrystalline barium titanate

Electrical conductivity of two types of lanthanum-doped barium titanote ceramics with different dopant levels was measured at temperatures between 900 and 1250° C andP _{O 2}from 10^–5 to 1 atm. The activation energies of the conduction for the two are interpreted in terms of the formation energy of ionized oxygen vacancies even in such a highP _{O 2}region. This fact is in contrast with a well -known controlled -valency model proposed for rare- earth -doped semi-conducting perovskites. In a lightly lanthanum-doped specimen, semiconduction achieved at elevated temperatures is retained on cooling the specimen to room temperature, whereas in a heavily doped specimen, the resultant high-temperature semiconduction changed to insulation on cooling. The former behaviour on cooling is successfully explained by a metastabilization of oxygen vacancies accompanied by electrons formed at elevated temperatures.     

Effect of Composition on the Oxygen Tracer Diffusion in Transparent Yttrium Aluminium Garnet (YAG) Ceramics

The grain boundary structure and oxygen tracer diffusion in transparent yttrium aluminum garnet (YAG) ceramics varying from 2% excess of Y₂O₃ to 0.5% excess of Al₂O₃ were studied. The characterization of the specimens is as follows: (i) For the Y₂O₃-excess specimen, a second phase (yttrium aluminum perovskite: YAP) containing silicon in the grain boundary was found, (ii) For the Al₂O₃-excess specimen, both aluminum-rich particles (alumina) and a silicon-rich segregant layer were observed in the grain boundary. The volume diffusion of the oxygen tracer is little influenced by the excess composition. In contrast, the grain boundary diffusion of the oxygen tracer is suppressed in the Y₂O₃-excess specimens, compared to Al₂O₃-excess specimens. These differences are thought to result from the chemical reaction between the second phase and the intergranular liquid phase during the sintering.     

Role of tungsten in promoting selective reduction of NO with CO over Ir/WO3–SiO2 catalysts

Catalytic hydrogenation of naphthalene to decalin was studied over a carbon-supported rhodium catalyst in supercritical carbon dioxide solvent at 333 K, and the results were compared with those in an organic solvent. cis-, trans-Decalin and tetralin were formed from the beginning of the reaction in supercritical carbon dioxide. Higher concentration of hydrogen in carbon dioxide solvent and on the active site, and also the suppression of desorption of partially hydrogenated tetralin molecules from the active site would be responsible for higher selectivity to cis-decalin in supercritical carbon dioxide than that in an organic solvent.     

Silica-supported cobalt catalysts for the selective reduction of nitrogen monoxide with propene

Catalytic behavior of silica-supported transition metals for NO reduction with propene in the presence of oxygen was investigated. While both silica and cobalt oxides did not show any activity for the selective NO reduction, impregnated CoO/SiO₂ prepared from cobalt acetate showed good activity although the preparation conditions had significant effect on the activity. It was suggested that highly dispersed surface Co²⁺ ions on silica are responsible for the catalytic activity.     

Preparation and reaction mechanistic characterization of sol–gel indium/alumina catalysts developed for NO x reduction by propene in lean conditions

The impregnation and sol–gel preparation methods were investigated to develop high activity catalysts and understand the significance of the indium–aluminium interaction on aluminasupported indium catalysts in NO _x reduction with propene. Active In/alumina catalysts with a very high surface area (270 m²/g) and thermal stability were prepared in controlled conditions by sol–gel processing. When Al isopropoxide and In nitrate in ethyl glycol were used as precursors in aqua media, indium atoms were incorporated evenly distributed as a thermally stable form in the aluminium oxide lattice structure. In wet impregnation it was beneficial to use a certain excess of aqueous In solution (volumes of solution : pores = 2 : 1) to have the highest NO _x reduction activity. The catalyst containing dispersed Al on In oxide (58 wt% In, phaseequilibrium preparation method) showed activity at lower temperatures than any other In–Al oxide catalyst or pure In₂O₃. The adsorption of different reaction intermediates on alumina and stable In₂O₃ sites were detected by FTIR studies. In/alumina catalysts have active sites to oxidize NO to NO₂, partially oxidize HC, form the actual reductant which contains N–H or N–C bonding and react with NO to dinitrogen. The cooperation with indium and aluminium was evident even in the mechanical mixture of sol–gel prepared alumina (301 m²/g) and In₂O₃ powders (27 m²/g), where the probability for molecularscale intimate contact between indium and aluminium sites was very low (particle size 10–250 m). Shortlived gaseous intermediates and surface migration are the possible reasons for the high catalytic activities on the two physically separated active sites both necessary for the reaction sequence.     

Synthesis of High Density and Transparent Forsterite Ceramics Using Nano-Sized Precursors and Their Dielectric Properties

Forsterite (Mg₂SiO₄) ceramics were prepared using Mg(OH)₂ and SiO₂ as precursors, and the effect of powder characteristics of Mg(OH)₂ on calcination and sintering was investigated. The use of highly dispersed Mg(OH)₂ powder (HD powder) resulted in a lower calcination temperature. Forsterite powder of high homogeneity and small particle size prepared from the HD powder enabled synthesis of high-density forsterite ceramics by ordinary sintering without applying external pressure. Moreover, transparent forsterite ceramics were successfully synthesized through addition of excess Mg to the precursors to compensate for Mg evaporated during the sintering process. Subsequent dielectric measurements revealed that the transparent forsterite ceramics had a very low dielectric loss (tan δ<10⁻⁴).     

三水铝石的粉碎机械力化学效就与热特性

使用振动球磨机将三水铝石粉体进行干式微粉碎.粉碎实验条件为介质球/试样(质量比)=8.5.研究调查了不同粉碎时间处理粉碎试样的机械力化学效应(平均粒径、结晶无定形和加热特性).结果表明,长时间粉碎,达到粉碎平衡,平均粒径趋于极限值.粉碎过程中未脱水.由于粉碎,加热脱水温度、结晶相变温度降低.     

Intestinal absorption and biological effects of orally administered amorphous silica particles

Although amorphous silica nanoparticles are widely used in the production of food products (e.g., as anticaking agents), there is little information available about their absorption and biological effects after oral exposure. Here, we examined the in vitro intestinal absorption and in vivo biological effects in mice of orally administered amorphous silica particles with diameters of 70, 300, and 1,000 nm (nSP70, mSP300, and mSP1000, respectively) and of nSP70 that had been surface-modified with carboxyl or amine groups (nSP70-C and nSP70-N, respectively). Analysis of intestinal absorption by means of the everted gut sac method combined with an inductively coupled plasma optical emission spectrometer showed that the intestinal absorption of nSP70-C was significantly greater than that of nSP70. The absorption of nSP70-N tended to be greater than that of nSP70; however, the results were not statistically significant. Our results indicate that silica nanoparticles can be absorbed through the intestine and that particle diameter and surface properties are major determinants of the degree of absorption. We also examined the biological effects of the silica particles after 28-day oral exposure in mice. Hematological, histopathological, and biochemical analyses showed no significant differences between control mice and mice treated with the silica particles, suggesting that the silica nanoparticles evaluated in this study are safe for use in food production.     

High Resistance of Cu–Ferrierite to Coke Formation During NH3-SCR in the Presence of n-Decane

Selective catalytic reduction of NO _x by NH₃ over Cu–FER and Cu–ZSM-5 in the presence of n-decane and SO₂ was investigated. NO _x conversion over Cu–ZSM-5 decreased in the presence of n-decane, owing to inhibition of the active sites by coke formation. In contrast, coke formation was negligible over Cu–FER, which maintained its NO _x conversion activity even in the presence of decane. Coke formation was negligible over H–ZSM-5 and H–FER supports, which suggests that Cu species were involved in coke formation. Temperature-programmed reduction by H₂ and electron spin resonance spectroscopy indicated that [Cu–O–Cu]²⁺ was probably the Cu species involved in coke formation over Cu–ZSM-5.